FDA NDC Directory · JSON-LD · Markdown

Amphetamine Sulfate

NDC 70010-041 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212619
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE SULFATE (10 mg/1)
Marketing started20190815
Package count1

External sources

Source: openFDA. Public-domain (CC0).